NCT06142331

Brief Summary

Aim: In this study, the types of home-based exercise programs prepared for patients receiving physiotherapy services in different rehabilitation institutions; It is aimed to examine the applicability and effectiveness advantages according to disease status, age, gender, socioeconomic level, education level, confidence in the home program, and functional independence level. Study type: observational study Research question; To what extent do patients participate in home-based exercise programs?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
237

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 16, 2023

Completed
1 day until next milestone

Study Start

First participant enrolled

November 17, 2023

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 21, 2023

Completed
10 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2023

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 17, 2024

Completed
Last Updated

June 4, 2024

Status Verified

June 1, 2024

Enrollment Period

14 days

First QC Date

November 16, 2023

Last Update Submit

June 3, 2024

Conditions

Keywords

home exerciseexercise behaviorexercise compliance

Outcome Measures

Primary Outcomes (1)

  • Vizuel Analog Scala, (VAS)

    VAS is an extremely simple, effective and repeatable measurement tool that requires minimal tools to measure both pain intensity and pain relief. It is a 10 cm long ruler drawn horizontally or vertically, starting with "No pain" and ending with "Unbearable pain". The patient is told to make a mark on this line that corresponds to the severity of his pain, intersecting this line. The distance from the lowest VAS level to the patient's mark is measured with a ruler to obtain a numerical index of the patient's pain intensity in cm or mm.

    baseline, post-exercise (day 12)

Secondary Outcomes (1)

  • Fatigue Severity Scale, (FSS)

    baseline, post-exercise (day 12)

Other Outcomes (4)

  • Functional independence measure, (FIM)

    baseline, post-exercise (day 12)

  • State Anxiety Scale

    baseline, post-exercise (day 12)

  • Functional Independence Measure for Children (WeeFIM)

    baseline, post-exercise (day 12)

  • +1 more other outcomes

Eligibility Criteria

AgeUp to 78 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Population/Sample of the Study: The population of the study consists of patients receiving Physiotherapy and Rehabilitation services in the hospital and rehabilitation center where the health services where the research will be carried out are provided. The sample of the research: Consists of 60 volunteer participants under the age of 18 and 177 participants over the age of 18 in the relevant units of three different health institutions, as stated, consisting of women and men. Only 89 female and male volunteer participants over the age of 18 will be included in the study in the physical therapy and rehabilitation unit of our hospital.

You may qualify if:

  • Having a clinical problem that causes physiotherapy and rehabilitation treatment
  • Being able to understand Turkish

You may not qualify if:

  • Not wanting to participate in the study
  • Having a chronic disease or disability that would prevent the application of the home program.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Necmettin Erbakan University

Konya, Meram, Turkey (Türkiye)

Location

Related Publications (1)

  • Kim JY, Lee MK, Lee DH, Kang DW, Min JH, Lee JW, Chu SH, Cho MS, Kim NK, Jeon JY. Effects of a 12-week home-based exercise program on quality of life, psychological health, and the level of physical activity in colorectal cancer survivors: a randomized controlled trial. Support Care Cancer. 2019 Aug;27(8):2933-2940. doi: 10.1007/s00520-018-4588-0. Epub 2018 Dec 18.

    PMID: 30564936BACKGROUND

Study Officials

  • Neslihan Altuntaş Yılmaz

    Necmettin Erbakan University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Target Duration
12 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
doctor

Study Record Dates

First Submitted

November 16, 2023

First Posted

November 21, 2023

Study Start

November 17, 2023

Primary Completion

December 1, 2023

Study Completion

January 17, 2024

Last Updated

June 4, 2024

Record last verified: 2024-06

Locations